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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40351Erstellt: 23. Oktober 2026

2-Methoxyethanol → Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate

https://huagongshe.com/de/reaction/40351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethoxyethanolHCID 8019—
EduktTriphenylphosphineHCID 11776—
EduktDi-tert-butyl azodicarboxylateHCID 97268—
EduktTert-butyl 2-(3-hydroxyquinolin-6-yl)acetateHCID 57691372—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetateHCID 5769092582%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A flask was charged with tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate (581.04 mg, 2.241 mmol) and triphenylphosphine (1.175 g, 4.482 mmol) then sealed with a septum and an placed under N2. Benzene (10 mL) was added, followed by 2-methoxyethanol (0.8838 ml, 11.20 mmol). The heterogeneous solution was cooled to 0° C., and di-tert-butyl azodicarboxylate (1.032 g, 4.482 mmol) was added as a solid in a single portion. The solution was allowed to warm to rt and maintained 20 h. The solution was then partitioned between saturated aqueous. NH4Cl, and the layers separated. The aqueous layer was extracted with EtOAc (2×50 mL), and the combined organic layers were washed with brine, dried (MgSO4), and concentrated in vacuo. The resulting residue was purified by MPLC (Teledine Isco combiFlash Companion), 80 g SiO2, solvent system: 90:10 hexanes:EtOAc gradient to 50:50 hexanes:EtOAc to give tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate (585. 2 mg, 82% yield). LRMS (ESI) m/z calcd for C18H24NO4 (M+H) 318.2. found 318.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524900B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-8dfdfb4c74224e3191f4dafaaac5c262
Quellennotizuspto-grants-2013_09